所有图片(1)
About This Item
经验公式（希尔记法）:
C18H13N3O
CAS号:
分子量:
287.32
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.25
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质量水平
方案
>98% (HPLC)
表单
solid
颜色
white
溶解性
DMSO: soluble 18 mg/mL (clear yellow solution)
H2O: insoluble
储存温度
2-8°C
SMILES字符串
O=C1N2CCc3c([nH]c4ccccc34)C2=Nc5ccccc15
InChI
1S/C18H13N3O/c22-18-13-6-2-4-8-15(13)20-17-16-12(9-10-21(17)18)11-5-1-3-7-14(11)19-16/h1-8,19H,9-10H2
InChI key
ACVGWSKVRYFWRP-UHFFFAOYSA-N
基因信息
human ... CYP1A1(1543) , CYP1A2(1544) , CYP1B1(1545)
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生化/生理作用
延迟整流 K + 通道阻滞剂。抑制血小板聚集；输精管扩张器。
警示用语：
Warning
危险声明
预防措施声明
危险分类
Acute Tox. 4 Oral
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Tiandong Bao et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 36(24), 3519-3522 (2012-03-01)
Develop an LC-MS method to determine evodiamine and rutaecarpine in rats plasma simultaneously. The method was employed to investigate pharmacokinetics of evodiamine and rutaecarpine. Blood samples were collected in different time after oral administrated with the extracts of Euodiae Fructus
Ben Liu et al.
Journal of chromatography. A, 1217(50), 7833-7839 (2010-11-12)
Evodiamine and rutaecarpine have been intensively studied due to their pharmacological actions and clinical applications. In this report, supercritical fluid was used to extract evodiamine and rutaecarpine from the unripe fruit of Evodia rutaecarpa. Response surface methodology using Box-Behnken experimental
Chongliang Lin et al.
Die Pharmazie, 66(12), 920-923 (2012-02-09)
A sensitive and selective liquid chromatography-mass spectrometry (LC-MS) method for the determination of evodiamine and rutecarpine in rabbit plasma was developed and validated. The analytes and internal standard (IS) are extracted from plasma by one-step protein precipitation with acetonitrile, and
Ming-Chung Tseng et al.
Organic letters, 13(16), 4434-4437 (2011-07-30)
Starting with commercial reagents, bicyclic 1,2,3-triazolium ionic liquids [b-3C-tr][NTf(2)] (1) and [b-4C-tr][NTf(2)] (2) were synthesized in four steps with high overall isolated yields of 68% and 76%, respectively. Since the C-5 hydrogen is acidic, under basic condition ionic liquids 1
Young Hwan Hong et al.
Biological & pharmaceutical bulletin, 33(10), 1704-1709 (2010-10-12)
A series of benzo-annulated rutaecarpines were prepared from anthranilic acid and 3-aminonaphthalene-2-carboxylic acid by Fischer indole synthesis as key reaction. Cytotoxicity was somewhat increased by the introduction of benzo-annulation, which was not directly related to the inhibitory activity against topoisomerases
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